A review and comparison of breast tumor cell nuclei segmentation performances using deep convolutional neural networks.

Journal: Scientific reports
Published Date:

Abstract

Breast cancer is currently the second most common cause of cancer-related death in women. Presently, the clinical benchmark in cancer diagnosis is tissue biopsy examination. However, the manual process of histopathological analysis is laborious, time-consuming, and limited by the quality of the specimen and the experience of the pathologist. This study's objective was to determine if deep convolutional neural networks can be trained, with transfer learning, on a set of histopathological images independent of breast tissue to segment tumor nuclei of the breast. Various deep convolutional neural networks were evaluated for the study, including U-Net, Mask R-CNN, and a novel network (GB U-Net). The networks were trained on a set of Hematoxylin and Eosin (H&E)-stained images of eight diverse types of tissues. GB U-Net demonstrated superior performance in segmenting sites of invasive diseases (AJI = 0.53, mAP = 0.39 & AJI = 0.54, mAP = 0.38), validated on two hold-out datasets exclusively containing breast tissue images of approximately 7,582 annotated cells. The results of the networks, trained on images independent of breast tissue, demonstrated that tumor nuclei of the breast could be accurately segmented.

Authors

  • Andrew Lagree
    Odette Cancer Program, Sunnybrook Health Sciences Centre, Toronto, Canada; Radiogenomics Laboratory, Sunnybrook Health Sciences Centre, Toronto, Canada.
  • Majidreza Mohebpour
    Biological Sciences Platform, Sunnybrook Research Institute, Toronto, Canada.
  • Nicholas Meti
    Division of Medical Oncology, 71545Sunnybrook Health Sciences Centre, Toronto, Canada.
  • Khadijeh Saednia
    Radiogenomics Laboratory, Sunnybrook Health Sciences Centre, Toronto, Canada; Department of Electrical Engineering and Computer Science, Lassonde School of Engineering, York University, Toronto, Canada.
  • Fang-I Lu
    Odette Cancer Program, Sunnybrook Health Sciences Centre, Toronto, Canada; Anatomic Pathology, Sunnybrook Health Sciences Centre, Toronto, Canada.
  • Elzbieta Slodkowska
    Department of Laboratory Medicine and Molecular Diagnostics, Sunnybrook Health Sciences Centre, Toronto, ON, Canada.
  • Sonal Gandhi
    Division of Medical Oncology, 71545Sunnybrook Health Sciences Centre, Toronto, Canada.
  • Eileen Rakovitch
    Department of Radiation Oncology, Sunnybrook Health Sciences Centre, Toronto, Canada; Department of Radiation Oncology, University of Toronto, Toronto, Canada.
  • Alex Shenfield
    Department of Engineering and Mathematics, Sheffield Hallam University, Sheffield, UK.
  • Ali Sadeghi-Naini
    Physical Sciences, Sunnybrook Research Institute, Sunnybrook Health Sciences Centre, Toronto, ON, Canada.
  • William T Tran
    Odette Cancer Program, Sunnybrook Health Sciences Centre, Toronto, Canada; Faculty of Medicine, Department Radiation Oncology, University of Toronto, Toronto, Canada; Faculty of Health and Wellbeing, Sheffield Hallam University, Sheffield, United Kingdom; Radiogenomics Laboratory, Sunnybrook Health Sciences Centre, Toronto, Canada. Electronic address: william.tran@sunnybrook.ca.